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SENTINEL CHOLINESTERASE LIQUID MODEL NUMBER 17.019A & 17.606

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K981800
510(k) Type
Traditional
Applicant
Equal Diagnostics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/6/1998
Days to Decision
46 days
Submission Type
Statement

SENTINEL CHOLINESTERASE LIQUID MODEL NUMBER 17.019A & 17.606

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K981800
510(k) Type
Traditional
Applicant
Equal Diagnostics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/6/1998
Days to Decision
46 days
Submission Type
Statement